Retinal telangiectasia-like lesions in a 15-year-old female with Hereditary hemorrhagic telangiectasia – a case report

Abstract Background Hereditary hemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome is a bleeding disorder that can affect all parts of the body including the eyes. Different ocular abnormalities have been described in relation to HHT, but the pathogenesis of retinal involvemen...

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Main Authors: Ardiana Ala, Torben Lykke Sørensen, Caroline Schmidt Laugesen
Format: Article
Language:English
Published: BMC 2022-11-01
Series:BMC Ophthalmology
Subjects:
Online Access:https://doi.org/10.1186/s12886-022-02658-7
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author Ardiana Ala
Torben Lykke Sørensen
Caroline Schmidt Laugesen
author_facet Ardiana Ala
Torben Lykke Sørensen
Caroline Schmidt Laugesen
author_sort Ardiana Ala
collection DOAJ
description Abstract Background Hereditary hemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome is a bleeding disorder that can affect all parts of the body including the eyes. Different ocular abnormalities have been described in relation to HHT, but the pathogenesis of retinal involvement is still unknown. A few cases have described chorioretinal abnormalities primarily occurring in elderly patients. In this study, we present a unique case of a young female with known HHT and a series of retinal fundus images including optical coherence tomography (OCT) and optical coherence tomography angiography (OCTA) with macular telangiectasia-like lesions. Case presentation A young female genetically diagnosed with hereditary hemorrhagic telangiectasia (HHT), is regularly attending retinal screening since she is diagnosed with Type 1 diabetes. At one visit, abnormal retinal telangiectasia-like lesions in the macula, are observed. These abnormalities are monitored over an extended period of time with fundus imaging, and further investigated with OCT and OCTA. The patient has no visual complaints at any time and best-corrected visual acuity is 20/20 Snellen equivalent in both eyes. Conclusions To the best of our knowledge, this is the first case to describe the occurrence of telangiectasia-like lesions in macula with secondary choriocapillaris atrophy in a patient diagnosed with HHT in such a young age.
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spelling doaj.art-e9834b15f071400c8a9f5c3948b6756f2022-12-22T04:14:25ZengBMCBMC Ophthalmology1471-24152022-11-012211510.1186/s12886-022-02658-7Retinal telangiectasia-like lesions in a 15-year-old female with Hereditary hemorrhagic telangiectasia – a case reportArdiana Ala0Torben Lykke Sørensen1Caroline Schmidt Laugesen2Department of Ophthalmology, Zealand University HospitalDepartment of Ophthalmology, Zealand University HospitalDepartment of Ophthalmology, Zealand University HospitalAbstract Background Hereditary hemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome is a bleeding disorder that can affect all parts of the body including the eyes. Different ocular abnormalities have been described in relation to HHT, but the pathogenesis of retinal involvement is still unknown. A few cases have described chorioretinal abnormalities primarily occurring in elderly patients. In this study, we present a unique case of a young female with known HHT and a series of retinal fundus images including optical coherence tomography (OCT) and optical coherence tomography angiography (OCTA) with macular telangiectasia-like lesions. Case presentation A young female genetically diagnosed with hereditary hemorrhagic telangiectasia (HHT), is regularly attending retinal screening since she is diagnosed with Type 1 diabetes. At one visit, abnormal retinal telangiectasia-like lesions in the macula, are observed. These abnormalities are monitored over an extended period of time with fundus imaging, and further investigated with OCT and OCTA. The patient has no visual complaints at any time and best-corrected visual acuity is 20/20 Snellen equivalent in both eyes. Conclusions To the best of our knowledge, this is the first case to describe the occurrence of telangiectasia-like lesions in macula with secondary choriocapillaris atrophy in a patient diagnosed with HHT in such a young age.https://doi.org/10.1186/s12886-022-02658-7Hereditary hemorrhagic telangiectasiaRendu-Osler-WeberRetinal telangiectasiaRetinal abnormalitiesCase report
spellingShingle Ardiana Ala
Torben Lykke Sørensen
Caroline Schmidt Laugesen
Retinal telangiectasia-like lesions in a 15-year-old female with Hereditary hemorrhagic telangiectasia – a case report
BMC Ophthalmology
Hereditary hemorrhagic telangiectasia
Rendu-Osler-Weber
Retinal telangiectasia
Retinal abnormalities
Case report
title Retinal telangiectasia-like lesions in a 15-year-old female with Hereditary hemorrhagic telangiectasia – a case report
title_full Retinal telangiectasia-like lesions in a 15-year-old female with Hereditary hemorrhagic telangiectasia – a case report
title_fullStr Retinal telangiectasia-like lesions in a 15-year-old female with Hereditary hemorrhagic telangiectasia – a case report
title_full_unstemmed Retinal telangiectasia-like lesions in a 15-year-old female with Hereditary hemorrhagic telangiectasia – a case report
title_short Retinal telangiectasia-like lesions in a 15-year-old female with Hereditary hemorrhagic telangiectasia – a case report
title_sort retinal telangiectasia like lesions in a 15 year old female with hereditary hemorrhagic telangiectasia a case report
topic Hereditary hemorrhagic telangiectasia
Rendu-Osler-Weber
Retinal telangiectasia
Retinal abnormalities
Case report
url https://doi.org/10.1186/s12886-022-02658-7
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AT carolineschmidtlaugesen retinaltelangiectasialikelesionsina15yearoldfemalewithhereditaryhemorrhagictelangiectasiaacasereport